7-Chloro-4-[(thiophen-2-yl)methyl]-2,3,4,5-tetrahydro-1,4-benzoxazepin-3-one CAS 1341001-70-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1341001-70-4
Molecular FormulaC14H12ClNO2S
Molecular Weight293.77 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

7-Chloro-4-[(thiophen-2-yl)methyl]-2,3,4,5-tetrahydro-1,4-benzoxazepin-3-one CAS 1341001-70-4 chemical structure

Description

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution, 7-Chloro-4-[(thiophen-2-yl)methyl]-2,3,4,5-tetrahydro-1,4-benzoxazepin-3-one is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 293.77 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

CATO supplies 7-Chloro-4-[(thiophen-2-yl)methyl]-2,3,4,5-tetrahydro-1,4-benzoxazepin-3-one (CAS 1341001-70-4), a certified reference material (molecular formula C14H12ClNO2S, MW 293.77 g/mol) for analytical method development and quality control.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

CATO manufactures 7-Chloro-4-[(thiophen-2-yl)methyl]-2,3,4,5-tetrahydro-1,4-benzoxazepin-3-one under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC14H12ClNO2S
Molecular Weight293.77 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Halogen ContentCl-containing
Nitrogen Atoms1
Sulfur Atoms1

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